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Journal ArticleDOI

Association of complement factor H Y402H gene polymorphism with different subtypes of exudative age-related macular degeneration.

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TLDR
The data suggest that the CFH Y402H polymorphism is a major risk factor for exudative AMD in a Central European population of Caucasoid descent.
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This article is published in Ophthalmology.The article was published on 2007-04-01. It has received 92 citations till now. The article focuses on the topics: Factor H & Gene polymorphism.

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Citations
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Do we need a new classification for choroidal neovascularization in age-related macular degeneration?

TL;DR: The introduction of intravitreal antivascular endothelial growth factor therapy for neovascular age-related macular degeneration (AMD) has not only improved the quality of life for patients but also raised the bar for what is considered effective treatment for this disease.
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Association of complement factor H and LOC387715 genotypes with response of exudative age-related macular degeneration to intravitreal bevacizumab.

TL;DR: The AMD-associated CFH Y402H and LOC387715 A69S variants were associated with differences in choroidal neovascular lesion size in this study, suggesting a potential pharmacogenetic relationship.
Journal ArticleDOI

Ocular blood flow in diabetes and age-related macular degeneration

TL;DR: The 2 leading causes of blindness in adults in the industrialized nations, diabetic retinopathy and age-related macular degeneration, have been investigated thoroughly with respect to their pathogenesis and knowledge of the pathophysiological vascular states underlying these diseases is essential for the assessment and development of future therapies.
Journal ArticleDOI

Oxidative stress, innate immunity, and age-related macular degeneration.

TL;DR: The background literature surrounding the known genetic and environmental contributors to AMD risk are highlighted, as well as a discussion of the potential mechanistic interplay of these factors that lead to disease pathogenesis with particular emphasis on the delicate control of inflammatory homeostasis and the centrality of the innate immune system in this process.
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Age-related maculopathy - linking aetiology and pathophysiological changes to the ischaemia hypothesis.

TL;DR: In this article, a linking hypothesis between aetiological factors including ischaemia and genetics and the development of early clinicopathological changes in age-related maculopathy is proposed.
References
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Journal ArticleDOI

Complement Factor H Polymorphism in Age-Related Macular Degeneration

TL;DR: A genome-wide screen for polymorphisms associated with age-related macular degeneration revealed a polymorphism in linkage disequilibrium with the risk allele representing a tyrosine-histidine change at amino acid 402 in the complement factor H gene.
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Complement factor H variant increases the risk of age-related macular degeneration.

TL;DR: DNA resequencing of the complement factor H gene within this haplotype revealed a common coding variant that significantly increases the risk for AMD with odds ratios between 2.45 and 5.57, which likely explains ∼43% of AMD in older adults.
Journal ArticleDOI

Complement Factor H Polymorphism and Age-Related Macular Degeneration

TL;DR: In this paper, single-nucleotide polymorphisms were tested for association with AMD in two independent case-control populations and significant association was identified within the regulation of complement activation locus and was centered over a tyrosine-402 --> histidine-402 protein polymorphism in the gene encoding complement factor.
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Photodynamic therapy of subfoveal choroidal neovascularization in age-related macular degeneration with verteporfin: two-year results of 2 randomized clinical trials-tap report 2.

TL;DR: To report 24-month vision and fluorescein angiographic outcomes from trials evaluating photodynamic therapy with verteporfin (Visudyne) in patients with subfoveal choroidal neovascularization caused by age-related macular degeneration (AMD).
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